Canonical Allele Identifier: CA1619235297
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622803C= , CM000668.2:g.31622803C= GRCh38
NC_000006.11:g.31590580C= , CM000668.1:g.31590580C= GRCh37
NC_000006.10:g.31698559C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000706625.1:c.30C= ENSP00000516471.1:p.Leu10=
ENST00000376033.3:c.14C= MANE Select ENSP00000365201.2:p.Ser5=
ENST00000376007.8:c.14C= ENSP00000365175.4:p.Ser5=
ENST00000376033.2:c.14C= ENSP00000365201.2:p.Ser5=
ENST00000469577.5:n.136-1458C=
NM_004638.3:c.14C= NP_004629.3:p.Ser5=
NM_080686.2:c.14C= NP_542417.2:p.Ser5=
XM_011514890.1:c.14C= XP_011513192.1:p.Ser5=
XM_017011274.1:c.14C= XP_016866763.1:p.Ser5=
NM_004638.4:c.14C= MANE Select NP_004629.3:p.Ser5=
NM_080686.3:c.14C= NP_542417.2:p.Ser5=